A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677652



Internal ID15067618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29087561..29128178hg38UCSC Ensembl
Innerchr15:29379764..29420381hg19UCSC Ensembl
Innerchr15:27167056..27207673hg18UCSC Ensembl
Innerchr15:27167056..27207673hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3840618
hg1940618
hg1840618
hg1740618
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515798
Supporting Variants
Samples
Known GenesAPBA2, FAM189A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677652
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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